A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411752



Internal ID22294431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1535233..1546063hg38UCSC Ensembl
chr10:1577428..1588258hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3810831
hg1910831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228287
Supporting Variants
SamplesNA19240
Known GenesADARB2, ADARB2-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14411752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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